A Pressure Relted Study Comparing a Compression Device and Profore® on Healthy Volunteers

PHASE1CompletedINTERVENTIONAL
Enrollment

12

Participants

Timeline

Start Date

May 31, 2008

Primary Completion Date

June 30, 2008

Study Completion Date

June 30, 2008

Conditions
Healthy Volunteers
Interventions
DEVICE

Compression Device

"The compression device will be worn for 8 hours each day on one leg. The device will be applied by the same clinician every morning.Interface pressure measurements will be made in both the sitting and standing position at three locations on the leg at the following time intervals:~* Immediately following device application~* 1 hour~* 4 hours~* 8 hours"

DEVICE

Profore®

"Profore® will be worn for 8 hours each day on opposite leg. Profore® will be applied by the same clinician every morning.Interface pressure measurements will be made in both the sitting and standing position at three locations on the leg at the following time intervals:~* Immediately following device application~* 1 hour~* 4 hours~* 8 hours"

Trial Locations (1)

Unknown

Hautarzt Phlebologe Allergologe, Freiburg im Breisgau

Sponsors

Lead Sponsor

All Listed Sponsors
lead

ConvaTec Inc.

INDUSTRY

NCT00821808 - A Pressure Relted Study Comparing a Compression Device and Profore® on Healthy Volunteers | Biotech Hunter | Biotech Hunter